A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360519



Internal ID22586188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78201616..78202151hg38UCSC Ensembl
chr10:79961373..79961908hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360519
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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